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Compound Detail

CHEMBL880

FAMCICLOVIR
💊 Approved Drug
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💊 Approved Drug
CC(=O)OCC(CCn1cnc2cnc(N)nc21)COC(C)=O

Basic Information

ChEMBL ID CHEMBL880
Name FAMCICLOVIR
Phase Approved
Structure Type MOL
InChI Key GGXKWVWZWMLJEH-UHFFFAOYSA-N
Therapeutic ✓ Yes
Active Moiety CHEMBL4594375

Known Names

BRL-42810 Famciclovir Famvir NSC-758921
0
Targets
3
Activities
1
Assay Types
15
PK Parameters
20
Publications
4
Known Names
9
Indications
1
Mechanisms

Molecular Properties

321.3
MW (Da)
0.54
ALogP
9
HBA
1
HBD
122.2
PSA (Ų)
0.73
QED
0
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
First Approval 1994
Availability Prescription
Chirality Achiral

Routes of Administration

Oral

Flags

Natural Product Prodrug
USAN Stem -vir
USAN Year 1992

Extended Properties

Molecular Formula C14H19N5O4
MW 321.34
Aromatic Rings 2
Heavy Atoms 23
NP-Likeness -0.20

Mechanism of Action

Mechanism Action Type Target Direct Efficacy
Human herpesvirus 1 DNA polymerase inhibitor INHIBITOR DNA polymerase catalytic subunit

Indications

Autoimmune Diseases Eye Infections Herpes Genitalis Herpes Labialis Herpes Zoster Virus Diseases Herpes Simplex Meniere Disease Multiple Sclerosis

ATC Classification

J05AB09
famciclovir
Level 1: ANTIINFECTIVES FOR SYSTEMIC USE
Level 2: ANTIVIRALS FOR SYSTEMIC USE
S01AD07
famciclovir
Level 1: SENSORY ORGANS
Level 2: OPHTHALMOLOGICALS

Activity Summary

IC50 3 meas.

Pharmacokinetic Data

Parameter Value Units Species
AUC 3160.0 ng.hr.mL-1 Homo sapiens
AUC 2110.0 ng.hr.mL-1 Homo sapiens
AUC 8770.0 ng.hr.mL-1 Homo sapiens
AUC 8940.0 ng.hr.mL-1 Homo sapiens
AUC 8540.0 ng.hr.mL-1 Homo sapiens
Cmax 2302.86 nM Homo sapiens
Cmax 2147.26 nM Homo sapiens
Cmax 10082.78 nM Homo sapiens
Cmax 10736.29 nM Homo sapiens
F 77.0 % Homo sapiens
T1/2 1.89 hr Homo sapiens
Tmax 1.02 hr Homo sapiens
Tmax 4.0 hr Homo sapiens
Tmax 1.0 hr Homo sapiens
Tmax 0.75 hr Homo sapiens

Literature References

PubMed DOI Target Context # Activities
- 10.6019/CHEMBL3885881 Rattus norvegicus 434
31158845 10.1038/s41586-019-1291-3 ADMET 104
- 10.5281/zenodo.13943903 ADMET 88
16472241 10.2174/1570163043334794 Hepatotoxicity 18
22194678 10.1371/journal.pcbi.1002310 Hepatotoxicity 14
20160046 10.1128/aac.01508-09 Homo sapiens 13
15646539 10.1016/s0399-8320(04)95062-2 Unchecked 11
15646539 10.1016/s0399-8320(04)95062-2 NON-PROTEIN TARGET 8
31158845 10.1038/s41586-019-1291-3 SGNH hydrolase-type esterase domain-containing protein 7
2754699 10.1021/jm00128a012 Mus musculus 6
19273678 10.1128/aac.01054-08 Homo sapiens 6
37468498 10.1038/s41467-023-40064-9 Alpha-1A adrenergic receptor 4
37468498 10.1038/s41467-023-40064-9 5-hydroxytryptamine receptor 2B 3
31158845 10.1038/s41586-019-1291-3 Acetyl esterase (Acetylxylosidase) 3
37468498 10.1038/s41467-023-40064-9 Muscarinic acetylcholine receptor M2 3
37468498 10.1038/s41467-023-40064-9 5-hydroxytryptamine receptor 2A 3
37468498 10.1038/s41467-023-40064-9 5-hydroxytryptamine receptor 1A 3
20014752 10.1021/tx900326k Hepatotoxicity 3
31158845 10.1038/s41586-019-1291-3 Acylhydrolase 3
37468498 10.1038/s41467-023-40064-9 Alpha-2A adrenergic receptor 3

Data from ChEMBL 36 via Core Engine